18-72173218-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173218
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173218
    reference: chr 18
allele count: 7
allele frequency: 5.838880269589443e-5
allele num: 119886
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000583399
  gene symbol: CNDP2
  hgvsc: ENST00000583399.1:n.556C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*206C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.339C>T
  hgvsp: ENST00000581272.1:c.339C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4511C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.339C>T
  hgvsp: ENST00000583785.1:c.339C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.384C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.222C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.210C>T
  hgvsp: ENST00000582666.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.339C>T
  hgvsp: ENST00000582589.1:c.339C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464014
  ensembl transcript: ENST00000584613
  gene symbol: CNDP2
  hgvsc: ENST00000584613.1:c.339C>T
  hgvsp: ENST00000584613.1:c.339C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.285C>T
  hgvsp: ENST00000580672.1:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.339C>T
  hgvsp: ENST00000583216.1:c.339C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.339C>T
  hgvsp: ENST00000581513.1:c.339C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.372C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.339C>T
  hgvsp: ENST00000579847.1:c.339C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.339C>T
  hgvsp: ENST00000324262.4:c.339C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4511C>T
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser113Ser
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

18-72173219-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173219
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173219
    reference: chr 18
allele count: 1
allele frequency: 8.343902276216541e-6
allele num: 119848
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.340G>A
  hgvsp: ENSP00000463222.1:p.Glu114Lys
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4512G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464014
  ensembl transcript: ENST00000584613
  gene symbol: CNDP2
  hgvsc: ENST00000584613.1:c.340G>A
  hgvsp: ENSP00000464014.1:p.Glu114Lys
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.385G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.223G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.373G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.286G>A
  hgvsp: ENSP00000464214.1:p.Glu96Lys
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.340G>A
  hgvsp: ENSP00000463702.1:p.Glu114Lys
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.340G>A
  hgvsp: ENSP00000462673.1:p.Glu114Lys
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*207G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.340G>A
  hgvsp: ENSP00000325548.4:p.Glu114Lys
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000583399
  gene symbol: CNDP2
  hgvsc: ENST00000583399.1:n.557G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.340G>A
  hgvsp: ENSP00000463182.1:p.Glu114Lys
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.211G>A
  hgvsp: ENSP00000461941.1:p.Glu71Lys
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.340G>A
  hgvsp: ENSP00000464151.1:p.Glu114Lys
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.340G>A
  hgvsp: ENSP00000462311.1:p.Glu114Lys
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4512G>A
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu114Lys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

18-72173227-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173227
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173227
    reference: chr 18
allele count: 1
allele frequency: 8.37436773523599e-6
allele num: 119412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*215C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4520C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464014
  ensembl transcript: ENST00000584613
  gene symbol: CNDP2
  hgvsc: ENST00000584613.1:c.348C>T
  hgvsp: ENST00000584613.1:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.219C>T
  hgvsp: ENST00000582666.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.348C>T
  hgvsp: ENST00000583785.1:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.294C>T
  hgvsp: ENST00000580672.1:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.348C>T
  hgvsp: ENST00000581272.1:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.348C>T
  hgvsp: ENST00000579847.1:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.381C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.393C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.348C>T
  hgvsp: ENST00000324262.4:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.348C>T
  hgvsp: ENST00000582589.1:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000583399
  gene symbol: CNDP2
  hgvsc: ENST00000583399.1:n.565C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4520C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.231C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.348C>T
  hgvsp: ENST00000583216.1:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.348C>T
  hgvsp: ENST00000581513.1:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28169
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe116Phe
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

18-72173230-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173230
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173230
    reference: chr 18
allele count: 3
allele frequency: 2.521559332291089e-5
allele num: 118974
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.297C>G
  hgvsp: ENST00000580672.1:c.297C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464014
  ensembl transcript: ENST00000584613
  gene symbol: CNDP2
  hgvsc: ENST00000584613.1:c.351C>G
  hgvsp: ENST00000584613.1:c.351C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.384C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.351C>G
  hgvsp: ENST00000579847.1:c.351C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.351C>G
  hgvsp: ENST00000324262.4:c.351C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.351C>G
  hgvsp: ENST00000581513.1:c.351C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.351C>G
  hgvsp: ENST00000583785.1:c.351C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.351C>G
  hgvsp: ENST00000583216.1:c.351C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.396C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.351C>G
  hgvsp: ENST00000581272.1:c.351C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.222C>G
  hgvsp: ENST00000582666.1:c.222C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4523C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*218C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.351C>G
  hgvsp: ENST00000582589.1:c.351C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.234C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4523C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000583399
  gene symbol: CNDP2
  hgvsc: ENST00000583399.1:n.568C>G
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr117Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

18-72173236-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173236
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173236
    reference: chr 18
allele count: 1
allele frequency: 8.444376889429329e-6
allele num: 118422
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.357G>A
  hgvsp: ENST00000581272.1:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.303G>A
  hgvsp: ENST00000580672.1:c.303G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.357G>A
  hgvsp: ENST00000583216.1:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.240G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.357G>A
  hgvsp: ENST00000583785.1:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*224G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464014
  ensembl transcript: ENST00000584613
  gene symbol: CNDP2
  hgvsc: ENST00000584613.1:c.357G>A
  hgvsp: ENST00000584613.1:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.357G>A
  hgvsp: ENST00000579847.1:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.357G>A
  hgvsp: ENST00000581513.1:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.357G>A
  hgvsp: ENST00000582589.1:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4529G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.228G>A
  hgvsp: ENST00000582666.1:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.357G>A
  hgvsp: ENST00000324262.4:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000583399
  gene symbol: CNDP2
  hgvsc: ENST00000583399.1:n.574G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4529G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.390G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.402G>A
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27417
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val119Val
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

18-72173237-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173237
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173237
    reference: chr 18
allele count: 1
allele frequency: 8.445945945945946e-6
allele num: 118400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.403G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.358G>A
  hgvsp: ENSP00000325548.4:p.Glu120Lys
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.241G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.391G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.358G>A
  hgvsp: ENSP00000463222.1:p.Glu120Lys
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464014
  ensembl transcript: ENST00000584613
  gene symbol: CNDP2
  hgvsc: ENST00000584613.1:c.358G>A
  hgvsp: ENSP00000464014.1:p.Glu120Lys
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.304G>A
  hgvsp: ENSP00000464214.1:p.Glu102Lys
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.358G>A
  hgvsp: ENSP00000463182.1:p.Glu120Lys
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4530G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.358G>A
  hgvsp: ENSP00000462673.1:p.Glu120Lys
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.229G>A
  hgvsp: ENSP00000461941.1:p.Glu77Lys
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000583399
  gene symbol: CNDP2
  hgvsc: ENST00000583399.1:n.575G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4530G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.358G>A
  hgvsp: ENSP00000464151.1:p.Glu120Lys
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.358G>A
  hgvsp: ENSP00000462311.1:p.Glu120Lys
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.358G>A
  hgvsp: ENSP00000463702.1:p.Glu120Lys
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*225G>A
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu120Lys
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

18-72173242-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173242
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173242
    reference: chr 18
allele count: 1
allele frequency: 8.475438180153914e-6
allele num: 117988
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.363A>G
  hgvsp: ENST00000579847.1:c.363A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*230A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.396A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.246A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.363A>G
  hgvsp: ENST00000581272.1:c.363A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.309A>G
  hgvsp: ENST00000580672.1:c.309A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000583399
  gene symbol: CNDP2
  hgvsc: ENST00000583399.1:n.580A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.363A>G
  hgvsp: ENST00000583785.1:c.363A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.363A>G
  hgvsp: ENST00000583216.1:c.363A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464014
  ensembl transcript: ENST00000584613
  gene symbol: CNDP2
  hgvsc: ENST00000584613.1:c.363A>G
  hgvsp: ENST00000584613.1:c.363A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4535A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.363A>G
  hgvsp: ENST00000582589.1:c.363A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.234A>G
  hgvsp: ENST00000582666.1:c.234A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.363A>G
  hgvsp: ENST00000581513.1:c.363A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.408A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.363A>G
  hgvsp: ENST00000324262.4:c.363A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4535A>G
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2441
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1750
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg121Arg
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

18-72173245-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173245
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173245
    reference: chr 18
allele count: 35
allele frequency: 2.987163730711457e-4
allele num: 117168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.366C>T
  hgvsp: ENST00000581272.1:c.366C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.366C>T
  hgvsp: ENST00000581513.1:c.366C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4538C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.366C>T
  hgvsp: ENST00000324262.4:c.366C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.366C>T
  hgvsp: ENST00000583216.1:c.366C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4538C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.399C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464014
  ensembl transcript: ENST00000584613
  gene symbol: CNDP2
  hgvsc: ENST00000584613.1:c.366C>T
  hgvsp: ENST00000584613.1:c.366C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.312C>T
  hgvsp: ENST00000580672.1:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*233C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.366C>T
  hgvsp: ENST00000583785.1:c.366C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000583399
  gene symbol: CNDP2
  hgvsc: ENST00000583399.1:n.583C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.249C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.411C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.366C>T
  hgvsp: ENST00000582589.1:c.366C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.237C>T
  hgvsp: ENST00000582666.1:c.237C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.366C>T
  hgvsp: ENST00000579847.1:c.366C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.366C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

18-72173250-AGCGCCGC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173250
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173243
    reference: chr 18
allele count: 6
allele frequency: 5.144826876575604e-5
allele num: 116622
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.367+10_367+16delGCGCGCC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*234+10_*234+16delGCGCGCC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.367+10_367+16delGCGCGCC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.367+10_367+16delGCGCGCC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.238+10_238+16delGCGCGCC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.313+10_313+16delGCGCGCC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.367+10_367+16delGCGCGCC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.250+10_250+16delGCGCGCC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.367+10_367+16delGCGCGCC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000583399
  gene symbol: CNDP2
  hgvsc: ENST00000583399.1:n.589_595delGCGCCGC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.367+10_367+16delGCGCGCC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.400+10_400+16delGCGCGCC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+10_412+16delGCGCGCC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.367+10_367+16delGCGCGCC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27247
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2404
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.367+10_367+16delGCGCGCC
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: AGCGCCGC
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ

18-72173252-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173252
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173252
    reference: chr 18
allele count: 8
allele frequency: 6.891680019296704e-5
allele num: 116082
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.367+6C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.250+6C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000583399
  gene symbol: CNDP2
  hgvsc: ENST00000583399.1:n.590C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.367+6C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*234+6C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.313+6C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.400+6C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.238+6C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.367+6C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4545C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.367+6C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.367+6C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.367+6C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4545C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+6C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.367+6C>T
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27212
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.367+6C>T
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD

18-72173253-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173253
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173253
    reference: chr 18
allele count: 119
allele frequency: 1.025155065472088e-3
allele num: 116080
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.367+7G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.400+7G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000583399
  gene symbol: CNDP2
  hgvsc: ENST00000583399.1:n.591G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*234+7G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.367+7G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.238+7G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.313+7G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.367+7G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.250+7G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4546G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+7G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.367+7G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.367+7G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.367+7G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4546G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.367+7G>A
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2434
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
hgvs: c.367+7G>A
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP

18-72173255-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173255
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173255
    reference: chr 18
allele count: 10
allele frequency: 8.653513326410523e-5
allele num: 115560
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.367+9C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.367+9C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4548C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.367+9C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.313+9C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.238+9C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000583399
  gene symbol: CNDP2
  hgvsc: ENST00000583399.1:n.593C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4548C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.367+9C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*234+9C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.400+9C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.250+9C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.367+9C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+9C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.367+9C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.367+9C>T
  variant of: http://identifiers.org/hgnc/24437
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6965
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14010
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

18-72173256-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173256
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173256
    reference: chr 18
allele count: 12
allele frequency: 1.05322286195759e-4
allele num: 113936
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4549G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000583399
  gene symbol: CNDP2
  hgvsc: ENST00000583399.1:n.594G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+10G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.238+10G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.367+10G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.367+10G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.367+10G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.313+10G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.250+10G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*234+10G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.367+10G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.367+10G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4549G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.367+10G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.400+10G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.367+10G>A
  variant of: http://identifiers.org/hgnc/24437
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6990
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD

18-72173257-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173257
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173257
    reference: chr 18
allele count: 5
allele frequency: 4.391897826888955e-5
allele num: 113846
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.400+11C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+11C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.367+11C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4550C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.367+11C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4550C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.367+11C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.238+11C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.313+11C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.367+11C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.367+11C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000583399
  gene symbol: CNDP2
  hgvsc: ENST00000583399.1:n.595C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.367+11C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.250+11C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.367+11C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*234+11C>T
  variant of: http://identifiers.org/hgnc/24437
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3755
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

18-72173258-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173258
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173258
    reference: chr 18
allele count: 3
allele frequency: 2.634351949420443e-5
allele num: 113880
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000583399
  gene symbol: CNDP2
  hgvsc: ENST00000583399.1:n.596G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.367+12G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.367+12G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.367+12G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.367+12G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+12G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4551G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4551G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.238+12G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*234+12G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.400+12G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.313+12G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.367+12G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.367+12G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.250+12G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.367+12G>A
  variant of: http://identifiers.org/hgnc/24437
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6977
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

18-72173259-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173259
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173259
    reference: chr 18
allele count: 4
allele frequency: 3.516483516483517e-5
allele num: 113750
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.367+13C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.367+13C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.367+13C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4552C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.367+13C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.250+13C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.400+13C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4552C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+13C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.238+13C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.367+13C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.313+13C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000583399
  gene symbol: CNDP2
  hgvsc: ENST00000583399.1:n.597C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*234+13C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.367+13C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.367+13C>T
  variant of: http://identifiers.org/hgnc/24437
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2572
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25846
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13608
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1894
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum

18-72173260-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173260
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173260
    reference: chr 18
allele count: 102
allele frequency: 9.395379683873107e-4
allele num: 108564
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.238+14G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4553G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.367+14G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.367+14G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*234+14G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.250+14G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.313+14G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.367+14G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000583399
  gene symbol: CNDP2
  hgvsc: ENST00000583399.1:n.598G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+14G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4553G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.367+14G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.400+14G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.367+14G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.367+14G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.367+14G>A
  variant of: http://identifiers.org/hgnc/24437
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3814
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2549
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6842
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 24064
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 1.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/18-72173262-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173262
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173262
    reference: chr 18
allele count: 1
allele frequency: 9.222539887485013e-6
allele num: 108430
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.400+16C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000583399
  gene symbol: CNDP2
  hgvsc: ENST00000583399.1:n.600C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*234+16C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+16C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.367+16C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.313+16C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.367+16C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.367+16C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.367+16C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.250+16C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.367+16C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.367+16C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4555C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.238+16C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.367+16C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4555C>A
  variant of: http://identifiers.org/hgnc/24437
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6823
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2928
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

18-72173263-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173263
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173263
    reference: chr 18
allele count: 1
allele frequency: 9.242144177449168e-6
allele num: 108200
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+17T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4556T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.367+17T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.313+17T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.367+17T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.250+17T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.367+17T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000583399
  gene symbol: CNDP2
  hgvsc: ENST00000583399.1:n.601T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4556T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.367+17T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.367+17T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.400+17T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.367+17T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.367+17T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.238+17T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*234+17T>C
  variant of: http://identifiers.org/hgnc/24437
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2601
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12767
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6813
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

18-72173267-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173267
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173267
    reference: chr 18
allele count: 18
allele frequency: 1.695777513990165e-4
allele num: 106146
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.400+21C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.238+21C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.367+21C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.250+21C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4560C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.367+21C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.313+21C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4560C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.367+21C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.367+21C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.367+21C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+21C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.367+21C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*234+21C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.367+21C>T
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3770
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6663
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23025
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1651
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD

18-72173268-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173268
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173268
    reference: chr 18
allele count: 86
allele frequency: 8.119641980437328e-4
allele num: 105916
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.367+22G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.238+22G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.367+22G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+22G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.367+22G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.367+22G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.367+22G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.313+22G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4561G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4561G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.367+22G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.367+22G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*234+22G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.250+22G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.400+22G>T
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 6593
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12192
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3827
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2998
  bin: 3.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

18-72173268-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173268
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173268
    reference: chr 18
allele count: 2
allele frequency: 1.888288832659844e-5
allele num: 105916
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.367+22G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.367+22G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+22G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*234+22G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.238+22G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.400+22G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4561G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.250+22G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.367+22G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4561G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.313+22G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.367+22G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.367+22G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.367+22G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.367+22G>A
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3827
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

18-72173270-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173270
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173269
    reference: chr 18
allele count: 23913
allele frequency: 2.103943409174893e-1
allele num: 113658
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.250+27delC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4566delC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.367+27delC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.238+27delC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+27delC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*234+27delC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.367+27delC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.400+27delC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.367+27delC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.313+27delC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.367+27delC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.367+27delC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.367+27delC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.367+27delC
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4566delC
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 7.25e1
  variant carriers: 1015
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 8.25e1
  variant carriers: 495
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 6.25e1
  variant carriers: 1711
genotype depth: GenotypeDepth
  all individuals: 17246
  bin: 2.25e1
  variant carriers: 650
genotype depth: GenotypeDepth
  all individuals: 2961
  bin: 7.5e0
  variant carriers: 670
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 7.75e1
  variant carriers: 740
genotype depth: GenotypeDepth
  all individuals: 9481
  bin: 2.75e1
  variant carriers: 747
genotype depth: GenotypeDepth
  all individuals: 2628
  bin: 4.25e1
  variant carriers: 1979
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 3.75e1
  variant carriers: 1575
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 2.5e0
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 3.25e1
  variant carriers: 1136
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 5.25e1
  variant carriers: 2328
genotype quality: GenotypeQuality
num of homozygotes: 2697
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: GC
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

18-72173274-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173274
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173274
    reference: chr 18
allele count: 1
allele frequency: 8.81197018029291e-6
allele num: 113482
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4567A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.367+28A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.367+28A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.367+28A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4567A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.367+28A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.250+28A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.367+28A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.400+28A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.238+28A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.313+28A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+28A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*234+28A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.367+28A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.367+28A>G
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5512
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9569
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: A
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

18-72173275-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173275
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173275
    reference: chr 18
allele count: 3
allele frequency: 2.644523192468398e-5
allele num: 113442
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+29G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.400+29G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.367+29G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.250+29G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.367+29G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.367+29G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.313+29G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.367+29G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*234+29G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.367+29G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.367+29G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4568G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4568G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.367+29G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.238+29G>A
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5504
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ

18-72173275-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173275
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173275
    reference: chr 18
allele count: 6
allele frequency: 5.289046384936796e-5
allele num: 113442
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.367+29G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4568G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.367+29G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*234+29G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.367+29G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.367+29G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.400+29G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+29G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.367+29G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.250+29G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.313+29G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4568G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.238+29G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.367+29G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.367+29G>T
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4081
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

18-72173275-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173275
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173274
    reference: chr 18
allele count: 1
allele frequency: 8.815077308227993e-6
allele num: 113442
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.238+30delA
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*234+30delA
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4569delA
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.367+30delA
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.250+30delA
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.400+30delA
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+30delA
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4569delA
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.367+30delA
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.367+30delA
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.367+30delA
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.367+30delA
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.367+30delA
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.313+30delA
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.367+30delA
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4081
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: GA
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

18-72173278-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173278
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173278
    reference: chr 18
allele count: 23812
allele frequency: 2.109683706919465e-1
allele num: 112870
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.367+32G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.367+32G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.367+32G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.238+32G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.367+32G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+32G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.400+32G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.313+32G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.367+32G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*234+32G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4571G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.250+32G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4571G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.367+32G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.367+32G>A
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2866
  bin: 4.25e1
  variant carriers: 2202
genotype depth: GenotypeDepth
  all individuals: 9426
  bin: 2.75e1
  variant carriers: 866
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 8.25e1
  variant carriers: 397
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 6.75e1
  variant carriers: 1254
genotype depth: GenotypeDepth
  all individuals: 5517
  bin: 3.25e1
  variant carriers: 1322
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 5.25e1
  variant carriers: 2302
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 5.75e1
  variant carriers: 2049
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 7.75e1
  variant carriers: 527
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 6.25e1
  variant carriers: 1593
genotype depth: GenotypeDepth
  all individuals: 3235
  bin: 7.5e0
  variant carriers: 746
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 3.75e1
  variant carriers: 1880
genotype depth: GenotypeDepth
  all individuals: 2751
  bin: 4.75e1
  variant carriers: 2459
genotype quality: GenotypeQuality
num of homozygotes: 2693
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

18-72173282-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173282
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173282
    reference: chr 18
allele count: 3
allele frequency: 2.686679443320019e-5
allele num: 111662
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.367+36G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.367+36G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.367+36G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.367+36G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4575G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.400+36G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.238+36G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*234+36G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+36G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4575G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.313+36G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.367+36G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.367+36G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.367+36G>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.250+36G>T
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7824
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12086
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP

18-72173283-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173283
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173283
    reference: chr 18
allele count: 3
allele frequency: 2.690679486259597e-5
allele num: 111496
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.367+37G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.250+37G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.367+37G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.367+37G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.313+37G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4576G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.367+37G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.367+37G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.238+37G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.367+37G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+37G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4576G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.400+37G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*234+37G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.367+37G>A
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7805
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

18-72173293-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72173293
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72173293
    reference: chr 18
allele count: 53
allele frequency: 4.783220822352984e-4
allele num: 110804
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.313+47T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.204+4586T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.367+47T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.367+47T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.204+4586T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.367+47T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*234+47T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.238+47T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.400+47T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.367+47T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.367+47T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+47T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.250+47T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.367+47T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.367+47T>C
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4628
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11127
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7514
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4094
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 6.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP

18-72176032-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176032
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176032
    reference: chr 18
allele count: 1
allele frequency: 8.320159747067144e-6
allele num: 120190
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.368-43C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.368-43C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2786C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.314-43C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.368-43C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1731C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.368-43C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-2016C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.251-43C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-2016C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.239-43C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.368-43C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.401-43C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.368-43C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*235-43C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.368-43C>G
  variant of: http://identifiers.org/hgnc/24437
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4314
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7753
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

18-72176041-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176041
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176041
    reference: chr 18
allele count: 1
allele frequency: 8.308822307526131e-6
allele num: 120354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.314-34C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.239-34C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-2007C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.368-34C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.368-34C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1740C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2795C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*235-34C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.368-34C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.251-34C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.368-34C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.368-34C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.368-34C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.368-34C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-2007C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.401-34C>T
  variant of: http://identifiers.org/hgnc/24437
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8044
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

18-72176042-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176042
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176042
    reference: chr 18
allele count: 1
allele frequency: 8.303992559622666e-6
allele num: 120424
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.401-33A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.314-33A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2796A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.239-33A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-2006A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.368-33A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1741A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.368-33A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.368-33A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.368-33A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-2006A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.368-33A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*235-33A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.368-33A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.368-33A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.251-33A>G
  variant of: http://identifiers.org/hgnc/24437
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3279
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1750
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

18-72176048-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176048
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176048
    reference: chr 18
allele count: 1
allele frequency: 8.29393713195654e-6
allele num: 120570
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2802T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.368-27T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.314-27T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.239-27T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1747T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.368-27T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.401-27T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-2000T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.368-27T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.251-27T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.368-27T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-2000T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.368-27T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*235-27T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.368-27T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.368-27T>C
  variant of: http://identifiers.org/hgnc/24437
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19204
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22388
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

18-72176058-GTGGATTGC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176058
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176050
    reference: chr 18
allele count: 1
allele frequency: 8.275542461808372e-6
allele num: 120838
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.368-14_368-7delGATTGCTG
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.368-14_368-7delGATTGCTG
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.368-14_368-7delGATTGCTG
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.368-14_368-7delGATTGCTG
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.251-14_251-7delGATTGCTG
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.368-14_368-7delGATTGCTG
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.368-14_368-7delGATTGCTG
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.401-14_401-7delGATTGCTG
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*235-14_*235-7delGATTGCTG
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.239-14_239-7delGATTGCTG
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.314-14_314-7delGATTGCTG
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.368-14_368-7delGATTGCTG
  variant of: http://identifiers.org/hgnc/24437
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: GTGGATTGC
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

18-72176071-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176071
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176071
    reference: chr 18
allele count: 32
allele frequency: 2.642356982428326e-4
allele num: 121104
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1977C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.314-4C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.401-4C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.239-4C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*235-4C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.368-4C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.368-4C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1770C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.368-4C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.368-4C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1977C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.368-4C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.251-4C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.368-4C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2825C>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.368-4C>G
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23113
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19844
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.368-4C>G
num of homozygotes: 1
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

18-72176072-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176072
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176072
    reference: chr 18
allele count: 1
allele frequency: 8.257092842751923e-6
allele num: 121108
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2826T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.368-3T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.368-3T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.251-3T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.368-3T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.368-3T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463702
  ensembl transcript: ENST00000581513
  gene symbol: CNDP2
  hgvsc: ENST00000581513.1:c.368-3T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.401-3T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1771T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.368-3T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.368-3T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.239-3T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1976T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.314-3T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*235-3T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1976T>C
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.368-3T>C
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD

18-72176083-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176083
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176083
    reference: chr 18
allele count: 27495
allele frequency: 2.269163475505084e-1
allele num: 121168
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1965T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.247T>C
  hgvsp: ENSP00000461941.1:p.Tyr83His
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.376T>C
  hgvsp: ENSP00000325548.4:p.Tyr126His
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.376T>C
  hgvsp: ENSP00000462311.1:p.Tyr126His
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*243T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2837T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.376T>C
  hgvsp: ENSP00000462673.1:p.Tyr126His
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1782T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.376T>C
  hgvsp: ENSP00000463182.1:p.Tyr126His
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.409T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.376T>C
  hgvsp: ENSP00000464151.1:p.Tyr126His
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1965T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.322T>C
  hgvsp: ENSP00000464214.1:p.Tyr108His
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.376T>C
  hgvsp: ENSP00000463222.1:p.Tyr126His
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  hgvsc: ENST00000584581.1:n.4T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.259T>C
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 7.75e1
  variant carriers: 1539
genotype depth: GenotypeDepth
  all individuals: 2914
  bin: 9.75e1
  variant carriers: 2862
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 4.75e1
  variant carriers: 1975
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 4.25e1
  variant carriers: 1585
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 5.25e1
  variant carriers: 2209
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 6.75e1
  variant carriers: 2015
genotype quality: GenotypeQuality
hgvs: p.Tyr126His
num of homozygotes: 3447
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

18-72176087-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176087
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176087
    reference: chr 18
allele count: 1
allele frequency: 8.249463784853985e-6
allele num: 121220
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.251G>A
  hgvsp: ENSP00000461941.1:p.Gly84Glu
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.380G>A
  hgvsp: ENSP00000462311.1:p.Gly127Glu
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.380G>A
  hgvsp: ENSP00000325548.4:p.Gly127Glu
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*247G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.380G>A
  hgvsp: ENSP00000463182.1:p.Gly127Glu
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.326G>A
  hgvsp: ENSP00000464214.1:p.Gly109Glu
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.413G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.380G>A
  hgvsp: ENSP00000463222.1:p.Gly127Glu
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1786G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1961G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.380G>A
  hgvsp: ENSP00000462673.1:p.Gly127Glu
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.263G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.380G>A
  hgvsp: ENSP00000464151.1:p.Gly127Glu
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2841G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1961G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  hgvsc: ENST00000584581.1:n.8G>A
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18664
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly127Glu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

18-72176091-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176091
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176091
    reference: chr 18
allele count: 1
allele frequency: 8.249327679794096e-6
allele num: 121222
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*251A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.384A>G
  hgvsp: ENST00000324262.4:c.384A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  hgvsc: ENST00000584581.1:n.12A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.384A>G
  hgvsp: ENST00000583216.1:c.384A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.384A>G
  hgvsp: ENST00000583785.1:c.384A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.330A>G
  hgvsp: ENST00000580672.1:c.330A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.267A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.417A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.255A>G
  hgvsp: ENST00000582666.1:c.255A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1957A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2845A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463182
  ensembl transcript: ENST00000582589
  gene symbol: CNDP2
  hgvsc: ENST00000582589.1:c.384A>G
  hgvsp: ENST00000582589.1:c.384A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.384A>G
  hgvsp: ENST00000581272.1:c.384A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1957A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.384A>G
  hgvsp: ENST00000579847.1:c.384A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1790A>G
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg128Arg
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

18-72176097-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176097
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176097
    reference: chr 18
allele count: 2
allele frequency: 1.649947201689546e-5
allele num: 121216
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1951G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.390G>A
  hgvsp: ENST00000581272.1:c.390G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.390G>A
  hgvsp: ENST00000583785.1:c.390G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.336G>A
  hgvsp: ENST00000580672.1:c.336G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1796G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*257G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.273G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.390G>A
  hgvsp: ENST00000583216.1:c.390G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.261G>A
  hgvsp: ENST00000582666.1:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  hgvsc: ENST00000584581.1:n.18G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.423G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1951G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.390G>A
  hgvsp: ENST00000579847.1:c.390G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.390G>A
  hgvsp: ENST00000324262.4:c.390G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2851G>A
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9607
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser130Ser
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS

18-72176097-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176097
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176097
    reference: chr 18
allele count: 1
allele frequency: 8.249736008447729e-6
allele num: 121216
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.336G>C
  hgvsp: ENST00000580672.1:c.336G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.261G>C
  hgvsp: ENST00000582666.1:c.261G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2851G>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*257G>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.390G>C
  hgvsp: ENST00000579847.1:c.390G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.390G>C
  hgvsp: ENST00000581272.1:c.390G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  hgvsc: ENST00000584581.1:n.18G>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.390G>C
  hgvsp: ENST00000583216.1:c.390G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1951G>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.423G>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.273G>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.390G>C
  hgvsp: ENST00000583785.1:c.390G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.390G>C
  hgvsp: ENST00000324262.4:c.390G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1796G>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1951G>C
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26906
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9607
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser130Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/18-72176099-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176099
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176099
    reference: chr 18
allele count: 2
allele frequency: 1.650110557407346e-5
allele num: 121204
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.263C>A
  hgvsp: ENSP00000461941.1:p.Thr88Asn
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.425C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.392C>A
  hgvsp: ENSP00000464151.1:p.Thr131Asn
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.338C>A
  hgvsp: ENSP00000464214.1:p.Thr113Asn
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  hgvsc: ENST00000584581.1:n.20C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1798C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.392C>A
  hgvsp: ENSP00000463222.1:p.Thr131Asn
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.392C>A
  hgvsp: ENSP00000325548.4:p.Thr131Asn
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.275C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*259C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.392C>A
  hgvsp: ENSP00000462311.1:p.Thr131Asn
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1949C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1949C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2853C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.392C>A
  hgvsp: ENSP00000462673.1:p.Thr131Asn
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26926
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9606
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr131Asn
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

18-72176100-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176100
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176100
    reference: chr 18
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2854T>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*260T>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000461941
  ensembl transcript: ENST00000582666
  gene symbol: CNDP2
  hgvsc: ENST00000582666.1:c.264T>G
  hgvsp: ENST00000582666.1:c.264T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1799T>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.393T>G
  hgvsp: ENST00000583216.1:c.393T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1948T>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.339T>G
  hgvsp: ENST00000580672.1:c.339T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  hgvsc: ENST00000584581.1:n.21T>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.276T>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.393T>G
  hgvsp: ENST00000579847.1:c.393T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.393T>G
  hgvsp: ENST00000581272.1:c.393T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.393T>G
  hgvsp: ENST00000583785.1:c.393T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1948T>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.426T>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.393T>G
  hgvsp: ENST00000324262.4:c.393T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: synonymous
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26931
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr131Thr
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum

18-72176100-TGATGATAAGGGCC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176100
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176087
    reference: chr 18
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsp: ENSP00000464214.1:p.Asp114ArgfsTer6
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsp: ENSP00000325548.4:p.Asp132ArgfsTer6
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsp: ENSP00000462311.1:p.Asp132ArgfsTer6
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsp: ENSP00000463222.1:p.Asp132ArgfsTer6
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsp: ENSP00000462673.1:p.Asp132ArgfsTer6
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18680
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp132ArgfsTer6
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: TGATGATAAGGGCC
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

18-72176102-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176102
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176102
    reference: chr 18
allele count: 1
allele frequency: 8.251505899826718e-6
allele num: 121190
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.395A>G
  hgvsp: ENSP00000462673.1:p.Asp132Gly
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.395A>G
  hgvsp: ENSP00000464151.1:p.Asp132Gly
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*262A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.278A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1801A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2856A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.428A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.395A>G
  hgvsp: ENSP00000463222.1:p.Asp132Gly
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.341A>G
  hgvsp: ENSP00000464214.1:p.Asp114Gly
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1946A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.395A>G
  hgvsp: ENSP00000462311.1:p.Asp132Gly
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  hgvsc: ENST00000584581.1:n.23A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1946A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.395A>G
  hgvsp: ENSP00000325548.4:p.Asp132Gly
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26941
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9596
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp132Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

18-72176102-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176102
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176102
    reference: chr 18
allele count: 1
allele frequency: 8.251505899826718e-6
allele num: 121190
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.395A>T
  hgvsp: ENSP00000325548.4:p.Asp132Val
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.395A>T
  hgvsp: ENSP00000463222.1:p.Asp132Val
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.341A>T
  hgvsp: ENSP00000464214.1:p.Asp114Val
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1946A>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1801A>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.395A>T
  hgvsp: ENSP00000462311.1:p.Asp132Val
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.395A>T
  hgvsp: ENSP00000464151.1:p.Asp132Val
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1946A>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  hgvsc: ENST00000584581.1:n.23A>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.395A>T
  hgvsp: ENSP00000462673.1:p.Asp132Val
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*262A>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2856A>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.278A>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.428A>T
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26941
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp132Val
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

18-72176104-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176104
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176104
    reference: chr 18
allele count: 1
allele frequency: 8.251914444151043e-6
allele num: 121184
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.397G>A
  hgvsp: ENSP00000463222.1:p.Asp133Asn
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1944G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*264G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464151
  ensembl transcript: ENST00000581272
  gene symbol: CNDP2
  hgvsc: ENST00000581272.1:c.397G>A
  hgvsp: ENSP00000464151.1:p.Asp133Asn
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.430G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  hgvsc: ENST00000584581.1:n.25G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.343G>A
  hgvsp: ENSP00000464214.1:p.Asp115Asn
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.397G>A
  hgvsp: ENSP00000325548.4:p.Asp133Asn
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.397G>A
  hgvsp: ENSP00000462311.1:p.Asp133Asn
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.397G>A
  hgvsp: ENSP00000462673.1:p.Asp133Asn
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2858G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.280G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1803G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1944G>A
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp133Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

18-72176114-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176114
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176114
    reference: chr 18
allele count: 1
allele frequency: 8.256683785524381e-6
allele num: 121114
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1934C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.353C>T
  hgvsp: ENSP00000464214.1:p.Pro118Leu
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.407C>T
  hgvsp: ENSP00000463222.1:p.Pro136Leu
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.407C>T
  hgvsp: ENSP00000462673.1:p.Pro136Leu
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.407C>T
  hgvsp: ENSP00000325548.4:p.Pro136Leu
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1934C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  hgvsc: ENST00000584581.1:n.35C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.290C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2868C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.440C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.407C>T
  hgvsp: ENSP00000462311.1:p.Pro136Leu
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*274C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1813C>T
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26930
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18572
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro136Leu
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

18-72176115-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176115
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176115
    reference: chr 18
allele count: 6
allele frequency: 4.954010271314629e-5
allele num: 121114
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.441G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1933G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.408G>A
  hgvsp: ENST00000583216.1:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.291G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.354G>A
  hgvsp: ENST00000580672.1:c.354G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1814G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.408G>A
  hgvsp: ENST00000583785.1:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.408G>A
  hgvsp: ENST00000579847.1:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.408G>A
  hgvsp: ENST00000324262.4:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1933G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  hgvsc: ENST00000584581.1:n.36G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*275G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2869G>A
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9579
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18572
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro136Pro
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD

18-72176121-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176121
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176121
    reference: chr 18
allele count: 12
allele frequency: 9.91014799154334e-5
allele num: 121088
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.414C>T
  hgvsp: ENST00000324262.4:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.447C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2875C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1820C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.414C>T
  hgvsp: ENST00000579847.1:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.414C>T
  hgvsp: ENST00000583216.1:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.414C>T
  hgvsp: ENST00000583785.1:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.360C>T
  hgvsp: ENST00000580672.1:c.360C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*281C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  hgvsc: ENST00000584581.1:n.42C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.297C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1927C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1927C>T
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9557
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala138Ala
num of homozygotes: 1
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD

18-72176122-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176122
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176122
    reference: chr 18
allele count: 3
allele frequency: 2.477659767760691e-5
allele num: 121082
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1821G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.415G>A
  hgvsp: ENSP00000325548.4:p.Gly139Ser
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.415G>A
  hgvsp: ENSP00000462673.1:p.Gly139Ser
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.298G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1926G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.415G>A
  hgvsp: ENSP00000463222.1:p.Gly139Ser
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.448G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1926G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*282G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.361G>A
  hgvsp: ENSP00000464214.1:p.Gly121Ser
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2876G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  hgvsc: ENST00000584581.1:n.43G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.415G>A
  hgvsp: ENSP00000462311.1:p.Gly139Ser
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9561
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly139Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

18-72176122-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176122
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176122
    reference: chr 18
allele count: 1
allele frequency: 8.258865892535638e-6
allele num: 121082
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*282G>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1821G>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.448G>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1926G>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.415G>C
  hgvsp: ENSP00000463222.1:p.Gly139Arg
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1926G>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.415G>C
  hgvsp: ENSP00000462311.1:p.Gly139Arg
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.361G>C
  hgvsp: ENSP00000464214.1:p.Gly121Arg
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.415G>C
  hgvsp: ENSP00000462673.1:p.Gly139Arg
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  hgvsc: ENST00000584581.1:n.43G>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2876G>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.415G>C
  hgvsp: ENSP00000325548.4:p.Gly139Arg
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.298G>C
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26967
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9561
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly139Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

18-72176131-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176131
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176131
    reference: chr 18
allele count: 1
allele frequency: 8.271435424903638e-6
allele num: 120898
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.424A>T
  hgvsp: ENSP00000462311.1:p.Asn142Tyr
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.307A>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.457A>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2885A>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1830A>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.424A>T
  hgvsp: ENSP00000325548.4:p.Asn142Tyr
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.370A>T
  hgvsp: ENSP00000464214.1:p.Asn124Tyr
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1917A>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.424A>T
  hgvsp: ENSP00000463222.1:p.Asn142Tyr
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1917A>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  hgvsc: ENST00000584581.1:n.52A>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.424A>T
  hgvsp: ENSP00000462673.1:p.Asn142Tyr
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*291A>T
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn142Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
reference allele: A
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/18-72176133-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176133
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176133
    reference: chr 18
allele count: 1
allele frequency: 8.271435424903638e-6
allele num: 120898
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1915C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.309C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.426C>A
  hgvsp: ENSP00000462311.1:p.Asn142Lys
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.426C>A
  hgvsp: ENSP00000325548.4:p.Asn142Lys
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2887C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.372C>A
  hgvsp: ENSP00000464214.1:p.Asn124Lys
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1832C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.426C>A
  hgvsp: ENSP00000462673.1:p.Asn142Lys
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.459C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.426C>A
  hgvsp: ENSP00000463222.1:p.Asn142Lys
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*293C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1915C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  hgvsc: ENST00000584581.1:n.54C>A
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9518
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn142Lys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

18-72176133-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176133
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176133
    reference: chr 18
allele count: 2
allele frequency: 1.654287084980728e-5
allele num: 120898
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.426C>T
  hgvsp: ENST00000583785.1:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.372C>T
  hgvsp: ENST00000580672.1:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1915C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.459C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1832C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.426C>T
  hgvsp: ENST00000324262.4:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.309C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2887C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.426C>T
  hgvsp: ENST00000583216.1:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.426C>T
  hgvsp: ENST00000579847.1:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*293C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1915C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  hgvsc: ENST00000584581.1:n.54C>T
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2154
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn142Asn
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

18-72176134-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176134
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176134
    reference: chr 18
allele count: 5
allele frequency: 4.138798755049334e-5
allele num: 120808
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1914G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.427G>A
  hgvsp: ENSP00000463222.1:p.Ala143Thr
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.427G>A
  hgvsp: ENSP00000462311.1:p.Ala143Thr
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.373G>A
  hgvsp: ENSP00000464214.1:p.Ala125Thr
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1833G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.427G>A
  hgvsp: ENSP00000325548.4:p.Ala143Thr
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*294G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1914G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.310G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.460G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  hgvsc: ENST00000584581.1:n.55G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2888G>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.427G>A
  hgvsp: ENSP00000462673.1:p.Ala143Thr
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9504
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18169
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala143Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

18-72176135-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176135
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176135
    reference: chr 18
allele count: 3
allele frequency: 2.483279253029601e-5
allele num: 120808
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1834C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.428C>T
  hgvsp: ENSP00000462311.1:p.Ala143Val
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1913C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1913C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.428C>T
  hgvsp: ENSP00000463222.1:p.Ala143Val
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.374C>T
  hgvsp: ENSP00000464214.1:p.Ala125Val
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.428C>T
  hgvsp: ENSP00000462673.1:p.Ala143Val
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.311C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.428C>T
  hgvsp: ENSP00000325548.4:p.Ala143Val
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  hgvsc: ENST00000584581.1:n.56C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*295C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.461C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2889C>T
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala143Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS

http://identifiers.org/exac.variant/18-72176137-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176137
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176137
    reference: chr 18
allele count: 12
allele frequency: 9.938546653194415e-5
allele num: 120742
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.313C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.430C>A
  hgvsp: ENSP00000462673.1:p.Leu144Met
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1911C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*297C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.430C>A
  hgvsp: ENSP00000462311.1:p.Leu144Met
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.463C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.376C>A
  hgvsp: ENSP00000464214.1:p.Leu126Met
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  hgvsc: ENST00000584581.1:n.58C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1836C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.430C>A
  hgvsp: ENSP00000325548.4:p.Leu144Met
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2891C>A
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.430C>A
  hgvsp: ENSP00000463222.1:p.Leu144Met
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1911C>A
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26797
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9460
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu144Met
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

18-72176137-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176137
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176137
    reference: chr 18
allele count: 12
allele frequency: 9.938546653194415e-5
allele num: 120742
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.430C>T
  hgvsp: ENST00000583216.1:c.430C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.430C>T
  hgvsp: ENST00000579847.1:c.430C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1911C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1836C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1911C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.430C>T
  hgvsp: ENST00000583785.1:c.430C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*297C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  hgvsc: ENST00000584581.1:n.58C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.313C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.430C>T
  hgvsp: ENST00000324262.4:c.430C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.463C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.376C>T
  hgvsp: ENST00000580672.1:c.376C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2891C>T
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9460
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26797
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu144Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

18-72176138-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176138
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176138
    reference: chr 18
allele count: 1
allele frequency: 8.288849839196314e-6
allele num: 120644
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.431T>C
  hgvsp: ENSP00000463222.1:p.Leu144Pro
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.464T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*298T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.377T>C
  hgvsp: ENSP00000464214.1:p.Leu126Pro
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1910T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.314T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.431T>C
  hgvsp: ENSP00000462673.1:p.Leu144Pro
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1837T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.431T>C
  hgvsp: ENSP00000325548.4:p.Leu144Pro
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1910T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2892T>C
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.431T>C
  hgvsp: ENSP00000462311.1:p.Leu144Pro
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  hgvsc: ENST00000584581.1:n.59T>C
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26767
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9450
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu144Pro
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

18-72176144-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176144
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176144
    reference: chr 18
allele count: 1
allele frequency: 8.304544246611745e-6
allele num: 120416
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.437C>T
  hgvsp: ENSP00000462311.1:p.Ala146Val
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.320C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1904C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*304C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1904C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.437C>T
  hgvsp: ENSP00000463222.1:p.Ala146Val
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.437C>T
  hgvsp: ENSP00000325548.4:p.Ala146Val
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.383C>T
  hgvsp: ENSP00000464214.1:p.Ala128Val
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1843C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.470C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2898C>T
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.437C>T
  hgvsp: ENSP00000462673.1:p.Ala146Val
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  hgvsc: ENST00000584581.1:n.65C>T
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17888
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26622
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala146Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP

18-72176150-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176150
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176150
    reference: chr 18
allele count: 1
allele frequency: 8.334027835652971e-6
allele num: 119990
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462311
  ensembl transcript: ENST00000579847
  gene symbol: CNDP2
  hgvsc: ENST00000579847.1:c.443A>G
  hgvsp: ENSP00000462311.1:p.Gln148Arg
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000462673
  ensembl transcript: ENST00000583216
  gene symbol: CNDP2
  hgvsc: ENST00000583216.1:c.443A>G
  hgvsp: ENSP00000462673.1:p.Gln148Arg
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000585263
  gene symbol: CNDP2
  hgvsc: ENST00000585263.1:n.1849A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464122
  ensembl transcript: ENST00000579583
  gene symbol: CNDP2
  hgvsc: ENST00000579583.1:c.205-1898A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584768
  gene symbol: CNDP2
  hgvsc: ENST00000584768.1:n.476A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000463222
  ensembl transcript: ENST00000583785
  gene symbol: CNDP2
  hgvsc: ENST00000583785.1:c.443A>G
  hgvsp: ENSP00000463222.1:p.Gln148Arg
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464214
  ensembl transcript: ENST00000580672
  gene symbol: CNDP2
  hgvsc: ENST00000580672.1:c.389A>G
  hgvsp: ENSP00000464214.1:p.Gln130Arg
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000577355
  gene symbol: CNDP2
  hgvsc: ENST00000577355.1:n.326A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000584581
  gene symbol: CNDP2
  hgvsc: ENST00000584581.1:n.71A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325548
  ensembl transcript: ENST00000324262
  gene symbol: CNDP2
  hgvsc: ENST00000324262.4:c.443A>G
  hgvsp: ENSP00000325548.4:p.Gln148Arg
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000325756
  ensembl transcript: ENST00000324301
  gene symbol: CNDP2
  hgvsc: ENST00000324301.8:c.205-1898A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000133313
  ensembl protein: ENSP00000464319
  ensembl transcript: ENST00000582260
  gene symbol: CNDP2
  hgvsc: ENST00000582260.1:c.*310A>G
  variant of: http://identifiers.org/hgnc/24437
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133313
  ensembl transcript: ENST00000582620
  gene symbol: CNDP2
  hgvsc: ENST00000582620.1:n.412+2904A>G
  variant of: http://identifiers.org/hgnc/24437
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26297
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln148Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

18-72176152-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72176152
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 72176152
allele count: 2
allele frequency: 1.6703135178473e-5
allele num: 119738
alternate allele: G
canonical: true
consequence: missense
filter: PASS
hgvs: p.Lys149Glu
num of homozygotes: 0
reference allele: A

GenotypeDepth
all individuals: 17033
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 200
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 995
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 681
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 411
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 95
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7977
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28444
bin: 2.25e1
variant carriers: 2

GenotypeDepth
all individuals: 21
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 645
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 34
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 161
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1123
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2872
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 1857
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3294
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8767
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32897
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2759
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4295
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160092807424594e-4
allele num: 8620
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518233990222573e-5
allele num: 65866
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.106747856343979e-4
allele num: 16094
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.12e0

DP
type: SiteQuality
SIO_000300: 1.547106e6

FS
type: SiteQuality
SIO_000300: 5.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.29e-1

QD
type: SiteQuality
SIO_000300: 1.012e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.64e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.143e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

GenotypeDepth
all individuals: 23
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 33
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 95
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28484
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7920
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 993
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2512
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 410
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16983
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 199
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1412
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3286
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2760
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4286
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8771
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2867
bin: 9.75e1
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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South Asian
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Latino
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Other
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MQ
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InbreedingCoeff
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MQRankSum
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DP
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FS
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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Latino
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Other
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European (Finnish)
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East Asian
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MQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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QD
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DP
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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Other
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South Asian
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Latino
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European (Finnish)
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FS
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MQ
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MQRankSum
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DP
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QD
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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European (Non-Finnish)
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Latino
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African
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South Asian
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MQ
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MQRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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QD
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ClippingRankSum
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VQSLOD
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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East Asian
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Other
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FS
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QD
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VQSLOD
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MQ
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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African
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European (Finnish)
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European (Non-Finnish)
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VQSLOD
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FS
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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MQ
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QD
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InbreedingCoeff
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MQRankSum
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SIO_000300: -2.87e-1

DP
type: SiteQuality
SIO_000300: 1.490349e6

GenotypeDepth
all individuals: 2076
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 982
bin: 4.25e1
variant carriers: 3

GenotypeDepth
all individuals: 7111
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 2423
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 14468
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 47
bin: 6.25e1
variant carriers: 2

GenotypeDepth
all individuals: 27285
bin: 2.25e1
variant carriers: 2

GenotypeDepth
all individuals: 202
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 24
bin: 7.25e1
variant carriers: 5

GenotypeDepth
all individuals: 97
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 7.75e1
variant carriers: 5

GenotypeDepth
all individuals: 3552
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 412
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1696
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 6.75e1
variant carriers: 4

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 21
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 361
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7990
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 939
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4153
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1402
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3141
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 871
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2894
bin: 9.75e1
variant carriers: 34

GenotypeQuality
all individuals: 1117
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5012
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2725
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28853
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 23
allele frequency: 3.547521362248203e-4
allele num: 64834
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.377465549851392e-4
allele num: 14804
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.990842126219391e-4
allele num: 10046
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.474031613687685e-4
allele num: 11514
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.149425287356322e-3
allele num: 870
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.57e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.71e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

QD
type: SiteQuality
SIO_000300: 1.208e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.24e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.68e0

DP
type: SiteQuality
SIO_000300: 1.478773e6

GenotypeDepth
all individuals: 3698
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 14169
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2084
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 417
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variant carriers: 0

GenotypeDepth
all individuals: 33
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variant carriers: 0

GenotypeDepth
all individuals: 17
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variant carriers: 0

GenotypeDepth
all individuals: 1942
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variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 982
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 7013
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variant carriers: 0

GenotypeDepth
all individuals: 97
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variant carriers: 0

GenotypeDepth
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1401
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5243
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2872
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 77
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variant carriers: 0

GenotypeQuality
all individuals: 3125
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variant carriers: 0

GenotypeQuality
all individuals: 1119
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
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variant carriers: 0

GenotypeQuality
all individuals: 1033
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1081
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2726
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28255
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4150
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7941
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14542
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 7.029053420805998e-4
allele num: 8536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9982
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64650
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.43e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.42e0

VQSLOD
type: SiteQuality
SIO_000300: 3.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.909999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.4e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.655e0

DP
type: SiteQuality
SIO_000300: 1.468759e6

FS
type: SiteQuality
SIO_000300: 1.0261e1

MQ
type: SiteQuality
SIO_000300: 5.106e1

GenotypeDepth
all individuals: 2023
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 268
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14093
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2062
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variant carriers: 0

GenotypeDepth
all individuals: 6973
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 420
bin: 4.75e1
variant carriers: 2

GenotypeDepth
all individuals: 12
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variant carriers: 1

GenotypeDepth
all individuals: 99
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variant carriers: 0

GenotypeDepth
all individuals: 23
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variant carriers: 1

GenotypeDepth
all individuals: 21
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variant carriers: 4

GenotypeDepth
all individuals: 3725
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variant carriers: 0

GenotypeDepth
all individuals: 991
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variant carriers: 0

GenotypeDepth
all individuals: 45
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variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 676
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variant carriers: 0

GenotypeQuality
all individuals: 2725
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
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variant carriers: 0

GenotypeQuality
all individuals: 212
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variant carriers: 0

GenotypeQuality
all individuals: 1064
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variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1119
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variant carriers: 0

GenotypeQuality
all individuals: 5222
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
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variant carriers: 0

GenotypeQuality
all individuals: 2874
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 426
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variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
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variant carriers: 0

GenotypeQuality
all individuals: 3114
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variant carriers: 0

GenotypeQuality
all individuals: 1102
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1400
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variant carriers: 0

GenotypeQuality
all individuals: 7892
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4145
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27952
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.010454362685967e-4
allele num: 9948
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14274
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.30925339787749e-5
allele num: 64452
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.28e-1

FS
type: SiteQuality
SIO_000300: 1.392e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

DP
type: SiteQuality
SIO_000300: 1.466869e6

MQ
type: SiteQuality
SIO_000300: 5.956e1

VQSLOD
type: SiteQuality
SIO_000300: 2.04e0

QD
type: SiteQuality
SIO_000300: 1.222e1

GenotypeDepth
all individuals: 425
bin: 4.75e1
variant carriers: 6

GenotypeDepth
all individuals: 16
bin: 8.75e1
variant carriers: 5

GenotypeDepth
all individuals: 1009
bin: 4.25e1
variant carriers: 5

GenotypeDepth
all individuals: 2049
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 109
bin: 5.75e1
variant carriers: 11

GenotypeDepth
all individuals: 27143
bin: 2.25e1
variant carriers: 7

GenotypeDepth
all individuals: 273
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variant carriers: 0

GenotypeDepth
all individuals: 2010
bin: 1.75e1
variant carriers: 14

GenotypeDepth
all individuals: 6962
bin: 3.25e1
variant carriers: 5

GenotypeDepth
all individuals: 3745
bin: 1.25e1
variant carriers: 7

GenotypeDepth
all individuals: 20
bin: 9.75e1
variant carriers: 3

GenotypeDepth
all individuals: 40
bin: 6.75e1
variant carriers: 7

GenotypeDepth
all individuals: 14074
bin: 2.75e1
variant carriers: 5

GenotypeQuality
all individuals: 112
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2720
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variant carriers: 0

GenotypeQuality
all individuals: 422
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variant carriers: 1

GenotypeQuality
all individuals: 1118
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1057
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7877
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variant carriers: 0

GenotypeQuality
all individuals: 5294
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4145
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1109
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3109
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27935
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1401
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2981
bin: 9.75e1
variant carriers: 118

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.152073732718894e-3
allele num: 868
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9942
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.610511660285416e-4
allele num: 11492
num of homozygotes: 0

South Asian
type: Population
allele count: 86
allele frequency: 6.014827248566233e-3
allele num: 14298
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 28
allele frequency: 4.345262112418138e-4
allele num: 64438
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.530456075910621e-4
allele num: 6534
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.75e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.447e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.65e-1

FS
type: SiteQuality
SIO_000300: 6.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.04e-1

QD
type: SiteQuality
SIO_000300: 1.213e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.469621e6

GenotypeDepth
all individuals: 26
bin: 7.25e1
variant carriers: 2

GenotypeDepth
all individuals: 12
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3767
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 49
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variant carriers: 0

GenotypeDepth
all individuals: 457
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variant carriers: 1

GenotypeDepth
all individuals: 211
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variant carriers: 1

GenotypeDepth
all individuals: 14
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variant carriers: 0

GenotypeDepth
all individuals: 5
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variant carriers: 1

GenotypeDepth
all individuals: 32
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variant carriers: 1

GenotypeDepth
all individuals: 107
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variant carriers: 1

GenotypeQuality
all individuals: 2893
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 514
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27591
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1123
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2725
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variant carriers: 0

GenotypeQuality
all individuals: 1162
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1401
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
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variant carriers: 0

GenotypeQuality
all individuals: 3105
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variant carriers: 0

GenotypeQuality
all individuals: 58
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variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 859
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variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5262
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7852
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variant carriers: 0

GenotypeQuality
all individuals: 4146
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1170
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.111581305619516e-5
allele num: 64276
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 7.069278933548778e-4
allele num: 9902
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.133685261806249e-5
allele num: 14018
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

FS
type: SiteQuality
SIO_000300: 2.537e0

DP
type: SiteQuality
SIO_000300: 1.466487e6

MQ
type: SiteQuality
SIO_000300: 5.959e1

QD
type: SiteQuality
SIO_000300: 1.204e1

MQRankSum
type: SiteQuality
SIO_000300: -1.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.65e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e-1

GenotypeDepth
all individuals: 15
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13693
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 374
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 20
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variant carriers: 1

GenotypeDepth
all individuals: 256
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1979
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 121
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 32
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2660
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variant carriers: 0

GenotypeQuality
all individuals: 362
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variant carriers: 0

GenotypeQuality
all individuals: 4952
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variant carriers: 0

GenotypeQuality
all individuals: 875
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variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2884
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 385
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4035
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variant carriers: 0

GenotypeQuality
all individuals: 3004
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7489
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1165
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26039
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variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1194
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1386
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

African
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allele count: 1
allele frequency: 1.022494887525562e-4
allele num: 9780
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 6
allele frequency: 9.428032683846638e-5
allele num: 63640
num of homozygotes: 0

East Asian
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allele count: 5
allele frequency: 5.905976848570753e-4
allele num: 8466
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.77e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

BaseQRankSum
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MQRankSum
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VQSLOD
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ClippingRankSum
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SIO_000300: -4.58e-1

FS
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InbreedingCoeff
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SIO_000300: -1.6e-3

DP
type: SiteQuality
SIO_000300: 1.492929e6

QD
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SIO_000300: 1.192e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.571882171712408e-5
allele num: 63618
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6506
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 2.362948960302458e-4
allele num: 8464
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 2
allele frequency: 1.516070345664039e-4
allele num: 13192
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 3.1e-2

InbreedingCoeff
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SIO_000300: -1.5e-3

ClippingRankSum
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ReadPosRankSum
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FS
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DP
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MQ
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VQSLOD
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QD
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SIO_000300: 1.128e1

BaseQRankSum
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6500
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.141788934619372e-5
allele num: 63658
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.181753722524226e-4
allele num: 8462
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.37e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

InbreedingCoeff
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SIO_000300: -1.4e-3

FS
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: -6.71e-1

ReadPosRankSum
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BaseQRankSum
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SIO_000300: -1.919e0

VQSLOD
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QD
type: SiteQuality
SIO_000300: 1.279e1

DP
type: SiteQuality
SIO_000300: 1.498696e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8464
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.572030434509212e-5
allele num: 63612
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13126
num of homozygotes: 0

African
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allele count: 3
allele frequency: 3.069995906672124e-4
allele num: 9772
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.05e-1

DP
type: SiteQuality
SIO_000300: 1.5011e6

VQSLOD
type: SiteQuality
SIO_000300: 9.69e-1

MQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: -2.1e-2

FS
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InbreedingCoeff
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SIO_000300: -1.5e-3

QD
type: SiteQuality
SIO_000300: 1.304e1

MQ
type: SiteQuality
SIO_000300: 5.964e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e0

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.480881399870383e-5
allele num: 61720
num of homozygotes: 0

Latino
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allele frequency: 5.765904285988853e-4
allele num: 10406
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African
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allele frequency: 9.735449735449736e-3
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Other
type: Population
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VQSLOD
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FS
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QD
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MQ
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BaseQRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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Other
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East Asian
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South Asian
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European (Finnish)
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European (Non-Finnish)
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VQSLOD
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ClippingRankSum
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MQRankSum
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MQ
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DP
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BaseQRankSum
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QD
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InbreedingCoeff
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FS
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 2842
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1086
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.266464032421479e-4
allele num: 7896
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11776
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61550
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9454
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.38e-1

DP
type: SiteQuality
SIO_000300: 1.575228e6

MQ
type: SiteQuality
SIO_000300: 5.961e1

FS
type: SiteQuality
SIO_000300: 5.845e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.66e-1

QD
type: SiteQuality
SIO_000300: 1.566e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.16e0

GenotypeDepth
all individuals: 713
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variant carriers: 0

GenotypeDepth
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variant carriers: 3

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
all individuals: 85
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GenotypeDepth
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GenotypeQuality
all individuals: 6755
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 19

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 22958
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11214
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7710
num of homozygotes: 0

African
type: Population
allele count: 13
allele frequency: 1.385632061394159e-3
allele num: 9382
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.646686866025556e-5
allele num: 60728
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 4.018485031143259e-4
allele num: 9954
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6368
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.39e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.07e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e-1

DP
type: SiteQuality
SIO_000300: 1.588438e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.275e1

VQSLOD
type: SiteQuality
SIO_000300: 3.11e0

GenotypeDepth
all individuals: 154
bin: 6.75e1
variant carriers: 9

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 11

GenotypeDepth
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GenotypeDepth
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variant carriers: 6

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1320
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 86

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3826
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GenotypeQuality
all individuals: 22277
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9344
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.143665513989311e-4
allele num: 6362
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11112
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.005631536604988e-4
allele num: 9944
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 83
allele frequency: 1.368237117140879e-3
allele num: 60662
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7700
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.743e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.41e-1

MQ
type: SiteQuality
SIO_000300: 5.698e1

QD
type: SiteQuality
SIO_000300: 1.603e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.598102e6

VQSLOD
type: SiteQuality
SIO_000300: -5.15e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.382e0

GenotypeDepth
all individuals: 2998
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1924
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variant carriers: 0

GenotypeDepth
all individuals: 22667
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2738
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variant carriers: 0

GenotypeDepth
all individuals: 6593
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variant carriers: 0

GenotypeDepth
all individuals: 43
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variant carriers: 0

GenotypeDepth
all individuals: 154
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GenotypeDepth
all individuals: 47
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variant carriers: 0

GenotypeQuality
all individuals: 658
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variant carriers: 0

GenotypeQuality
all individuals: 6712
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GenotypeQuality
all individuals: 2566
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GenotypeQuality
all individuals: 1355
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GenotypeQuality
all individuals: 1003
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 653
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GenotypeQuality
all individuals: 1380
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1103
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GenotypeQuality
all individuals: 3826
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variant carriers: 0

GenotypeQuality
all individuals: 1320
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GenotypeQuality
all individuals: 1584
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 558
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2928
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variant carriers: 1

GenotypeQuality
all individuals: 2786
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1088
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.648478454386601e-5
allele num: 60662
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9944
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.999280057595392e-5
allele num: 11112
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9344
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7700
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.382e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.698e1

QD
type: SiteQuality
SIO_000300: 1.603e1

FS
type: SiteQuality
SIO_000300: 1.743e0

VQSLOD
type: SiteQuality
SIO_000300: -5.15e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.41e-1

DP
type: SiteQuality
SIO_000300: 1.598102e6

GenotypeDepth
all individuals: 4046
bin: 1.25e1
variant carriers: 1265

GenotypeDepth
all individuals: 2089
bin: 5.75e1
variant carriers: 2019

GenotypeDepth
all individuals: 405
bin: 9.75e1
variant carriers: 395

GenotypeDepth
all individuals: 2583
bin: 4.75e1
variant carriers: 2283

GenotypeDepth
all individuals: 1706
bin: 1.75e1
variant carriers: 937

GenotypeDepth
all individuals: 206
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variant carriers: 205

GenotypeDepth
all individuals: 1504
bin: 6.75e1
variant carriers: 1486

GenotypeDepth
all individuals: 323
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variant carriers: 316

GenotypeQuality
all individuals: 175
bin: 5.25e1
variant carriers: 63

GenotypeQuality
all individuals: 1042
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variant carriers: 80

GenotypeQuality
all individuals: 228
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variant carriers: 27

GenotypeQuality
all individuals: 2029
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GenotypeQuality
all individuals: 23060
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variant carriers: 20894

GenotypeQuality
all individuals: 2801
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variant carriers: 60

GenotypeQuality
all individuals: 854
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variant carriers: 91

GenotypeQuality
all individuals: 4807
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variant carriers: 33

GenotypeQuality
all individuals: 3275
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variant carriers: 45

GenotypeQuality
all individuals: 605
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variant carriers: 25

GenotypeQuality
all individuals: 1907
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variant carriers: 54

GenotypeQuality
all individuals: 866
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variant carriers: 70

GenotypeQuality
all individuals: 797
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variant carriers: 58

GenotypeQuality
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variant carriers: 92

GenotypeQuality
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variant carriers: 82

GenotypeQuality
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variant carriers: 19

GenotypeQuality
all individuals: 266
bin: 1.75e1
variant carriers: 42

GenotypeQuality
all individuals: 185
bin: 4.75e1
variant carriers: 72

GenotypeQuality
all individuals: 175
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variant carriers: 72

GenotypeQuality
all individuals: 473
bin: 3.75e1
variant carriers: 74

Latino
type: Population
allele count: 3905
allele frequency: 3.428446005267779e-1
allele num: 11390
num of homozygotes: 680

South Asian
type: Population
allele count: 3608
allele frequency: 2.735405610310842e-1
allele num: 13190
num of homozygotes: 487

European (Finnish)
type: Population
allele count: 775
allele frequency: 1.191574415744157e-1
allele num: 6504
num of homozygotes: 35

East Asian
type: Population
allele count: 2477
allele frequency: 2.929280983916746e-1
allele num: 8456
num of homozygotes: 340

Other
type: Population
allele count: 159
allele frequency: 1.901913875598086e-1
allele num: 836
num of homozygotes: 17

African
type: Population
allele count: 1343
allele frequency: 1.381118881118881e-1
allele num: 9724
num of homozygotes: 99

European (Non-Finnish)
type: Population
allele count: 11646
allele frequency: 1.832342112715944e-1
allele num: 63558
num of homozygotes: 1039

MQRankSum
type: SiteQuality
SIO_000300: 1.73e-1

FS
type: SiteQuality
SIO_000300: 1.849e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.98e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.48e-1

DP
type: SiteQuality
SIO_000300: 1.964974e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.85e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.7e-2

QD
type: SiteQuality
SIO_000300: 2.135e1

GenotypeDepth
all individuals: 318
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2104
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2693
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1655
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variant carriers: 0

GenotypeDepth
all individuals: 867
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variant carriers: 0

GenotypeDepth
all individuals: 427
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variant carriers: 0

GenotypeDepth
all individuals: 4075
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GenotypeDepth
all individuals: 251
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GenotypeQuality
all individuals: 302
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variant carriers: 0

GenotypeQuality
all individuals: 42
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GenotypeQuality
all individuals: 5355
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variant carriers: 0

GenotypeQuality
all individuals: 1985
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 896
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2333
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1303
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1403
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63492
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12964
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.177578897786152e-4
allele num: 8492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9714
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.118e1

MQ
type: SiteQuality
SIO_000300: 5.947e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.459e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.45e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.931e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.162e0

DP
type: SiteQuality
SIO_000300: 1.921562e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.4e-2

GenotypeDepth
all individuals: 3143
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variant carriers: 1

GenotypeDepth
all individuals: 868
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GenotypeDepth
all individuals: 4081
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 1813
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variant carriers: 0

GenotypeQuality
all individuals: 5344
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GenotypeQuality
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GenotypeQuality
all individuals: 376
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GenotypeQuality
all individuals: 41
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GenotypeQuality
all individuals: 410
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GenotypeQuality
all individuals: 2719
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GenotypeQuality
all individuals: 919
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GenotypeQuality
all individuals: 557
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GenotypeQuality
all individuals: 1070
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variant carriers: 0

GenotypeQuality
all individuals: 803
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GenotypeQuality
all individuals: 2331
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GenotypeQuality
all individuals: 468
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GenotypeQuality
all individuals: 3487
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variant carriers: 0

GenotypeQuality
all individuals: 334
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GenotypeQuality
all individuals: 16048
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3965
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1416
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16974
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1301
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 12948
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63476
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 3
allele frequency: 3.089598352214212e-4
allele num: 9710
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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SIO_000300: 1.1e-2

MQRankSum
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DP
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QD
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InbreedingCoeff
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SIO_000300: 4.8e-3

FS
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VQSLOD
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MQ
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SIO_000300: 5.963e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63476
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12948
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8492
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.235602094240838e-4
allele num: 11460
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9710
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.92078e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e-2

QD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 4.8e-3

MQRankSum
type: SiteQuality
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FS
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SIO_000300: 8.97e-1

ReadPosRankSum
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -2.451e0

MQ
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SIO_000300: 5.963e1

VQSLOD
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GenotypeDepth
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bin: 5.25e1
variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1301
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9710
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8492
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.723200494284832e-5
allele num: 12948
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63476
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.8e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.451e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

QD
type: SiteQuality
SIO_000300: 1.393e1

MQ
type: SiteQuality
SIO_000300: 5.963e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e-2

FS
type: SiteQuality
SIO_000300: 8.97e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.92078e6

GenotypeDepth
all individuals: 229
bin: 8.75e1
variant carriers: 224

GenotypeDepth
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GenotypeDepth
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variant carriers: 1299

GenotypeDepth
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variant carriers: 812

GenotypeDepth
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variant carriers: 283

GenotypeDepth
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variant carriers: 145

GenotypeDepth
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variant carriers: 683

GenotypeDepth
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variant carriers: 891

GenotypeQuality
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variant carriers: 77

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 58

GenotypeQuality
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GenotypeQuality
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variant carriers: 43

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 20887

GenotypeQuality
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GenotypeQuality
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variant carriers: 69

GenotypeQuality
all individuals: 328
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variant carriers: 87

GenotypeQuality
all individuals: 972
bin: 3.25e1
variant carriers: 89

European (Finnish)
type: Population
allele count: 777
allele frequency: 1.195384615384615e-1
allele num: 6500
num of homozygotes: 36

Latino
type: Population
allele count: 3908
allele frequency: 3.429273429273429e-1
allele num: 11396
num of homozygotes: 682

East Asian
type: Population
allele count: 2477
allele frequency: 2.936225699383594e-1
allele num: 8436
num of homozygotes: 341

European (Non-Finnish)
type: Population
allele count: 11610
allele frequency: 1.835457046194707e-1
allele num: 63254
num of homozygotes: 1035

African
type: Population
allele count: 1335
allele frequency: 1.381987577639752e-1
allele num: 9660
num of homozygotes: 99

South Asian
type: Population
allele count: 3544
allele frequency: 2.769615504845264e-1
allele num: 12796
num of homozygotes: 482

Other
type: Population
allele count: 161
allele frequency: 1.944444444444444e-1
allele num: 828
num of homozygotes: 18

MQRankSum
type: SiteQuality
SIO_000300: 1.31e-1

DP
type: SiteQuality
SIO_000300: 1.908219e6

FS
type: SiteQuality
SIO_000300: 2.076e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-2

MQ
type: SiteQuality
SIO_000300: 5.974e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.932e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.43e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.82e-2

QD
type: SiteQuality
SIO_000300: 2.24e1

GenotypeDepth
all individuals: 17018
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8781
bin: 9.75e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62914
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.631117347833714e-4
allele num: 11402
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8448
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6494
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12004
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.54e-1

MQ
type: SiteQuality
SIO_000300: 5.748e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-2

MQRankSum
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -3.0e-4

BaseQRankSum
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SIO_000300: -1.707e0

FS
type: SiteQuality
SIO_000300: 1.027e0

DP
type: SiteQuality
SIO_000300: 1.630266e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62862
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.551136363636364e-4
allele num: 8448
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11400
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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DP
type: SiteQuality
SIO_000300: 1.628654e6

ClippingRankSum
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VQSLOD
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MQRankSum
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QD
type: SiteQuality
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FS
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InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

BaseQRankSum
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SIO_000300: -3.139e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.15e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

GenotypeDepth
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variant carriers: 3

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3415
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 46
allele frequency: 7.34026935597115e-4
allele num: 62668
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.089280197713933e-4
allele num: 6474
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8428
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.788890841975742e-5
allele num: 11378
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 4.197271773347324e-4
allele num: 9530
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -1.9e-3

FS
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VQSLOD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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MQ
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SIO_000300: 6.0e1

QD
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SIO_000300: 1.594e1

DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 8.721437292865864e-5
allele num: 11466
num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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East Asian
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
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QD
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MQ
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FS
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.513179796023364e-5
allele num: 66086
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.642e0

VQSLOD
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QD
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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SIO_000300: -2.03e-1

BaseQRankSum
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SIO_000300: -3.067e0

ReadPosRankSum
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SIO_000300: 1.71e0

DP
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SIO_000300: 1.724438e6

MQ
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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num of homozygotes: 0

South Asian
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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VQSLOD
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QD
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BaseQRankSum
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MQ
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ClippingRankSum
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FS
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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African
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Other
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South Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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DP
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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MQRankSum
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FS
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MQ
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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African
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South Asian
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Latino
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ReadPosRankSum
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DP
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BaseQRankSum
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MQRankSum
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MQ
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FS
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QD
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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South Asian
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

East Asian
type: Population
allele count: 26
allele frequency: 3.006475485661424e-3
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66538
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.0e-2

FS
type: SiteQuality
SIO_000300: 2.032e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 9.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.82e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.39e-2

DP
type: SiteQuality
SIO_000300: 1.76513e6

QD
type: SiteQuality
SIO_000300: 1.348e1

MQ
type: SiteQuality
SIO_000300: 5.958e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.56e-1

GenotypeDepth
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bin: 1.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 90
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 1709
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.111111111111111e-3
allele num: 900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66540
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.88e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.668e0

MQRankSum
type: SiteQuality
SIO_000300: -6.28e-1

FS
type: SiteQuality
SIO_000300: 1.543e0

DP
type: SiteQuality
SIO_000300: 1.765506e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.215e0

QD
type: SiteQuality
SIO_000300: 8.83e0

GenotypeDepth
all individuals: 2484
bin: 5.75e1
variant carriers: 2301

GenotypeDepth
all individuals: 865
bin: 9.25e1
variant carriers: 840

GenotypeDepth
all individuals: 84
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variant carriers: 50

GenotypeDepth
all individuals: 14735
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variant carriers: 374

GenotypeDepth
all individuals: 1864
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variant carriers: 1779

GenotypeDepth
all individuals: 5173
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variant carriers: 727

GenotypeDepth
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variant carriers: 988

GenotypeDepth
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GenotypeDepth
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variant carriers: 1094

GenotypeDepth
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variant carriers: 169

GenotypeDepth
all individuals: 2407
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variant carriers: 2260

GenotypeDepth
all individuals: 1295
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variant carriers: 1257

GenotypeQuality
all individuals: 32
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variant carriers: 6

GenotypeQuality
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variant carriers: 19

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 8

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 379
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variant carriers: 40

GenotypeQuality
all individuals: 105
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variant carriers: 3

GenotypeQuality
all individuals: 40
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variant carriers: 7

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 12

GenotypeQuality
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variant carriers: 31

GenotypeQuality
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variant carriers: 7

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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variant carriers: 28

GenotypeQuality
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variant carriers: 23787

GenotypeQuality
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variant carriers: 42

GenotypeQuality
all individuals: 49
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variant carriers: 4

GenotypeQuality
all individuals: 26426
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variant carriers: 14

African
type: Population
allele count: 1164
allele frequency: 1.12095531587057e-1
allele num: 10384
num of homozygotes: 75

South Asian
type: Population
allele count: 4366
allele frequency: 2.645739910313901e-1
allele num: 16502
num of homozygotes: 618

Latino
type: Population
allele count: 4126
allele frequency: 3.574770403742852e-1
allele num: 11542
num of homozygotes: 770

European (Finnish)
type: Population
allele count: 933
allele frequency: 1.413208118751893e-1
allele num: 6602
num of homozygotes: 59

European (Non-Finnish)
type: Population
allele count: 14114
allele frequency: 2.118964688926255e-1
allele num: 66608
num of homozygotes: 1512

East Asian
type: Population
allele count: 2603
allele frequency: 3.017621145374449e-1
allele num: 8626
num of homozygotes: 392

Other
type: Population
allele count: 189
allele frequency: 2.09070796460177e-1
allele num: 904
num of homozygotes: 21

BaseQRankSum
type: SiteQuality
SIO_000300: 2.62e0

FS
type: SiteQuality
SIO_000300: 5.45e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.24e-2

MQ
type: SiteQuality
SIO_000300: 5.961e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.52e0

QD
type: SiteQuality
SIO_000300: 1.652e1

DP
type: SiteQuality
SIO_000300: 2.604106e6

GenotypeDepth
all individuals: 92
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2
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variant carriers: 0

GenotypeDepth
all individuals: 88
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variant carriers: 0

GenotypeDepth
all individuals: 113
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variant carriers: 0

GenotypeDepth
all individuals: 342
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
all individuals: 87
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GenotypeDepth
all individuals: 587
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GenotypeDepth
all individuals: 66
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GenotypeDepth
all individuals: 117
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GenotypeQuality
all individuals: 1993
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GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 46
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GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2848
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2184
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variant carriers: 0

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 1243
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66618
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.69438e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e-1

FS
type: SiteQuality
SIO_000300: 1.07e0

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.369e0

VQSLOD
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SIO_000300: 1.91e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.164e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 34
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GenotypeQuality
all individuals: 2180
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501095799933952e-5
allele num: 66618
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.273e1

VQSLOD
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SIO_000300: 2.76e0

DP
type: SiteQuality
SIO_000300: 1.694198e6

MQ
type: SiteQuality
SIO_000300: 5.946e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.38e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501140867058965e-5
allele num: 66616
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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QD
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VQSLOD
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BaseQRankSum
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MQ
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DP
type: SiteQuality
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MQRankSum
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FS
type: SiteQuality
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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DP
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQ
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FS
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ClippingRankSum
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VQSLOD
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QD
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.002462018855461e-5
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
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FS
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MQRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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ReadPosRankSum
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 1
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European (Non-Finnish)
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num of homozygotes: 0

Latino
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Other
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QD
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VQSLOD
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MQ
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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FS
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 9.63948332369385e-5
allele num: 10374
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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Other
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MQ
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InbreedingCoeff
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MQRankSum
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DP
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FS
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VQSLOD
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QD
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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East Asian
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Latino
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European (Finnish)
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Other
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QD
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MQRankSum
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InbreedingCoeff
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DP
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FS
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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FS
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InbreedingCoeff
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MQ
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DP
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VQSLOD
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GenotypeQuality
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East Asian
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African
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Latino
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South Asian
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VQSLOD
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QD
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InbreedingCoeff
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ClippingRankSum
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DP
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MQRankSum
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FS
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ReadPosRankSum
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MQ
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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East Asian
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Other
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VQSLOD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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FS
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QD
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MQRankSum
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ClippingRankSum
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DP
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

Latino
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Other
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African
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European (Non-Finnish)
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East Asian
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European (Finnish)
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MQ
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InbreedingCoeff
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MQRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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FS
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ReadPosRankSum
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

African
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European (Non-Finnish)
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allele num: 66540
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Other
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East Asian
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South Asian
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Latino
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ReadPosRankSum
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ClippingRankSum
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DP
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VQSLOD
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InbreedingCoeff
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MQRankSum
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FS
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MQ
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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South Asian
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Latino
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African
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East Asian
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European (Finnish)
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ReadPosRankSum
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VQSLOD
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QD
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InbreedingCoeff
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MQ
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FS
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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African
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Latino
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European (Finnish)
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East Asian
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ReadPosRankSum
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InbreedingCoeff
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MQ
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DP
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MQRankSum
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VQSLOD
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QD
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FS
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ClippingRankSum
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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South Asian
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European (Finnish)
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Latino
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African
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MQ
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ReadPosRankSum
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MQRankSum
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DP
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QD
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ClippingRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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Other
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African
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European (Finnish)
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South Asian
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BaseQRankSum
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MQRankSum
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DP
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FS
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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QD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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European (Finnish)
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Other
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European (Non-Finnish)
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East Asian
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BaseQRankSum
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FS
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VQSLOD
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MQRankSum
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ReadPosRankSum
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DP
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MQ
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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South Asian
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African
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European (Finnish)
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Latino
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Other
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VQSLOD
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ReadPosRankSum
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FS
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ClippingRankSum
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MQ
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QD
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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Latino
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South Asian
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Other
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East Asian
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European (Finnish)
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ReadPosRankSum
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QD
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MQ
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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DP
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BaseQRankSum
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MQRankSum
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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European (Finnish)
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Latino
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East Asian
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European (Non-Finnish)
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South Asian
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ClippingRankSum
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DP
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ReadPosRankSum
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FS
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BaseQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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MQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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Latino
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South Asian
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European (Finnish)
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MQ
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QD
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BaseQRankSum
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MQRankSum
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DP
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ClippingRankSum
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InbreedingCoeff
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FS
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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Other
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European (Finnish)
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Latino
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East Asian
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South Asian
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ClippingRankSum
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VQSLOD
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QD
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InbreedingCoeff
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MQ
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MQRankSum
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DP
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FS
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.850000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.058e0

GenotypeDepth
all individuals: 147
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 209
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 284
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2058
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41975
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1891
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2769
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1156
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7583
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511715797430083e-5
allele num: 66150
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.951e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.925e1

QD
type: SiteQuality
SIO_000300: 7.74e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.964e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.441e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.99e-1

FS
type: SiteQuality
SIO_000300: 1.4075e1

MQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

DP
type: SiteQuality
SIO_000300: 1.672583e6

GenotypeDepth
all individuals: 17504
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 335
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2100
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 573
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1132
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1444
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2020
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41263
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7469
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 642
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2760
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1861
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10246
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6490
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65920
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.721437292865864e-5
allele num: 11466
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.51e1

MQRankSum
type: SiteQuality
SIO_000300: 5.01e-1

DP
type: SiteQuality
SIO_000300: 1.659868e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.46e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.27e-1

MQ
type: SiteQuality
SIO_000300: 5.92e1